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Journal ArticleDOI

Copper-Catalyzed Rearrangement of (Z)-Propynal Hydrazones via N−N Bond Cleavage

Itaru Nakamura, +3 more
- 18 Aug 2010 - 
- Vol. 12, Iss: 18, pp 4198-4200
TLDR
Propynal hydrazones are successfully converted to the corresponding 3-aminoacrylonitriles in the presence of copper catalysts in good to high yields through C-N bond formation and subsequent β-elimination involving cleavage of N-N and C-H bonds.
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This article is published in Organic Letters.The article was published on 2010-08-18. It has received 18 citations till now. The article focuses on the topics: Propynal & Bond cleavage.

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Citations
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Copper-Catalyzed Rearrangement of (Z)-Propynal Hydrazones via N—N Bond Cleavage.

TL;DR: In this paper, a variety of β-aminoacrylonitriles is prepared in the reaction, catalyzed by Cu(OAc)2, followed by the Z/E-isomerization, induced by AcOH.
References
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Journal ArticleDOI

Gold-Catalyzed Organic Reactions

TL;DR: Important vinylgold intermediates, the transmetalation from gold to other transition metals, the development of new ligands for gold catalysis, and significant contributions from computational chemistry are other crucial points for the field highlighted here.
Journal ArticleDOI

Catalytic Carbophilic Activation: Catalysis by Platinum and Gold π Acids

TL;DR: The ability of platinum and gold catalysts to effect powerful atom-economic transformations has led to a marked increase in their utilization and the application of platinum- and gold-catalyzed transformations in natural product synthesis is discussed.
Journal ArticleDOI

Gold-catalyzed cycloisomerizations of enynes: a mechanistic perspective.

TL;DR: The proposed involvement of cyclopropyl metal carbenes of type 4 in the electrophilic activation of enynes by transition metals was first substantiated in reactions catalyzed by Pd(II), in which the initially formed cycloprostyl palladiumCarbenes undergo [4 + 2] cycloaddition with the double bond of the conjugate enyne.
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Gold-catalyzed organic transformations.

TL;DR: Thanks to gold-based catalysts, various organic transformations have been accessible under facile conditions with both high yields and chemoselectivity.
Journal ArticleDOI

Relativistic effects in homogeneous gold catalysis

TL;DR: This Review draws on experimental and computational data to present the current understanding of homogeneous gold catalysis, focusing on previously unexplored reactivity and its application to the development of new methodology.
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